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Journal Abstract Search

339 related items for PubMed ID: 16359140

  • 1. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA, Furze AD, Angeli SI.
    J Laryngol Otol; 2006 Mar; 120(3):230-2. PubMed ID: 16359140
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  • 4. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
    Howes T, Madden C, Dasgupta S, Saeed S, Das V.
    J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
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  • 5. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
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  • 6. Cochlear implantation in sudden bilateral sensorineural hearing loss.
    Sargent EW, Beck DL.
    Ear Nose Throat J; 1998 Apr 02; 77(4):300-3. PubMed ID: 9581397
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  • 7. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun 02; 28(3):332-42. PubMed ID: 17485982
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  • 9. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S.
    Laryngoscope; 2004 Jun 02; 114(6):1085-91. PubMed ID: 15179218
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  • 15. A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation.
    Mancuso M, Filosto M, Forli F, Rocchi A, Berrettini S, Siciliano G, Murri L.
    Acta Neurol Scand; 2004 Jul 02; 110(1):72-4. PubMed ID: 15180810
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  • 19. Cochlear implantation in patients with bilateral severe sensorineural hearing loss after major blunt head trauma.
    Greenberg SL, Shipp D, Lin VY, Chen JM, Nedzelski JM.
    Otol Neurotol; 2011 Jan 02; 32(1):48-54. PubMed ID: 21157292
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